| CPC A23L 27/36 (2016.08) [A23F 3/34 (2013.01); A23L 2/56 (2013.01); A23L 2/60 (2013.01); A23L 2/68 (2013.01); A23L 5/40 (2016.08); A23L 27/30 (2016.08); A23L 27/39 (2016.08); A23L 27/88 (2016.08); A61K 31/192 (2013.01); A61K 31/235 (2013.01); A61K 36/28 (2013.01); B01D 15/361 (2013.01); C07H 15/256 (2013.01); C07K 1/16 (2013.01); C07K 1/18 (2013.01); A23V 2002/00 (2013.01); A23V 2200/15 (2013.01); A23V 2250/258 (2013.01); A61K 2236/31 (2013.01); A61K 2236/39 (2013.01)] | 21 Claims |
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1. An aqueous steviol glycoside solution comprising:
a) greater than 0.3% by weight of a total steviol glycoside composition comprising rebaudioside M, rebaudioside D, or combinations thereof; and
b) a steviol glycoside solubility enhancer composition in an amount such that the aqueous solution comprises a 1:0.3 to 1:3 ratio by weight of steviol glycoside to solubility enhancer composition, the steviol glycoside solubility enhancer composition comprising
i) one or more monocaffeoylquinic acids or salts thereof; and
ii) at least 20% by weight of one or more dicaffeoylquinic acids or salts thereof;
wherein the steviol glycoside remains in solution for at least 7 days at about 25° C.
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